Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1053872
rs1053872
0.925 0.080 9 4860643 3 prime UTR variant G/C;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs1053872
rs1053872
0.925 0.080 9 4860643 3 prime UTR variant G/C;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10758657
rs10758657
9 4853751 intron variant A/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10758657
rs10758657
9 4853751 intron variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10815094
rs10815094
9 4845520 intron variant A/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10815094
rs10815094
9 4845520 intron variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs13284787
rs13284787
9 4811553 intron variant A/C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs13284787
rs13284787
9 4811553 intron variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs13300663
rs13300663
9 4814948 intron variant G/A;C snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2011 2011
dbSNP: rs13300663
rs13300663
9 4814948 intron variant G/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs13300663
rs13300663
9 4814948 intron variant G/A;C snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs457287
rs457287
9 4834394 intron variant A/G;T snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2013 2013
dbSNP: rs7044812
rs7044812
9 4864885 intron variant T/A;C;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7853365
rs7853365
9 4855858 intron variant A/C;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs7853365
rs7853365
9 4855858 intron variant A/C;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10974808
rs10974808
9 4840380 intron variant A/G snv 9.0E-02
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10974808
rs10974808
9 4840380 intron variant A/G snv 9.0E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10974815
rs10974815
9 4854253 intron variant C/T snv 0.11
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs10974815
rs10974815
9 4854253 intron variant C/T snv 0.11
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10758658
rs10758658
9 4856877 intron variant G/A snv 0.15
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.800 1.000 1 2009 2017
dbSNP: rs10758658
rs10758658
9 4856877 intron variant G/A snv 0.15
Finding of Mean Corpuscular Hemoglobin
0.800 1.000 1 2009 2017
dbSNP: rs10758658
rs10758658
9 4856877 intron variant G/A snv 0.15
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs3780359
rs3780359
9 4835574 intron variant G/A snv 0.16
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2236497
rs2236497
9 4844704 intron variant T/C snv 0.22 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2009 2009
dbSNP: rs2236497
rs2236497
9 4844704 intron variant T/C snv 0.22 0.19
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012